NR2F2 and TRIP4

  • Number of citations of the paper that reports this interaction (PMID 20211142)
  • 148
  • Data Source:
  • BioGRID (two hybrid)

NR2F2

TRIP4

Gene Name nuclear receptor subfamily 2, group F, member 2 thyroid hormone receptor interactor 4
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Prostate cancer (gene x gene interaction) ( 22219177)
  • Response to TNF-alpha inhibitors in rheumatoid arthritis ( 22569225)
  • Sex hormone-binding globulin levels ( 22829776)
Protein-Protein Interactions 19 interactors: BCL11A BCL11B BIK EP300 FAM46A HDAC1 HIPK3 LCK MYOD1 NCOR2 NR2F6 NR3C1 NSD1 PHB2 PIAS1 SETD7 SQSTM1 TRIM24 TRIP4 22 interactors: AR ASCC2 ASCC3 CREBBP EP300 ESR1 ESR2 GTF2A1 JUN NCOA1 NEK6 NFKB1 NR2F2 PAX9 PPARG RARA RELA RXRA SHD TBP THRB XBP1
Entrez ID 7026 9325
HPRD ID 00139 05140
Ensembl ID ENSG00000185551 ENSG00000103671
Uniprot IDs F1D8R0 P24468 Q15650
PDB IDs 3CJW 2E5O
Enriched GO Terms of Interacting Partners?
Tagcloud ?
akr1c4  anomalies  apparently  array  balanced  bases  cdon  cgh  chrna7  confirming  dd  diagnoses  dock8  gata3  id  indistinguishable  inherited  intellectual  karyotype  karyotyping  mb  mca  overlooked  prenatal  pws  rearrangements  spanning  tier  tp63 
abca7  bin1  cass4  cd2ap  cd33  celf1  chapter  discoveries  drb1  drb5  epha1  fermt2  inpp5d  mef2c  ms4a4  ms4a6  nme8  picalm  pld3  psen1  psen2  ptk2b  rin3  slc24a4  sorl1  touch  trem2  unsuspected  zcwpw1 
Tagcloud (Difference) ?
akr1c4  anomalies  apparently  array  balanced  bases  cdon  cgh  chrna7  confirming  dd  diagnoses  dock8  gata3  id  indistinguishable  inherited  intellectual  karyotype  karyotyping  mb  mca  overlooked  prenatal  pws  rearrangements  spanning  tier  tp63 
abca7  bin1  cass4  cd2ap  cd33  celf1  chapter  discoveries  drb1  drb5  epha1  fermt2  inpp5d  mef2c  ms4a4  ms4a6  nme8  picalm  pld3  psen1  psen2  ptk2b  rin3  slc24a4  sorl1  touch  trem2  unsuspected  zcwpw1 
Tagcloud (Intersection) ?